Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9AKS9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:0000154 | rRNA modification | 6 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008168 | methyltransferase activity | 4 | 11 |
GO:0008173 | RNA methyltransferase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0008649 | rRNA methyltransferase activity | 5 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016435 | rRNA (guanine) methyltransferase activity | 6 | 1 |
GO:0140102 | catalytic activity, acting on a rRNA | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 241 | 245 | PF00656 | 0.572 |
CLV_C14_Caspase3-7 | 69 | 73 | PF00656 | 0.573 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.641 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.641 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.295 |
DEG_APCC_DBOX_1 | 107 | 115 | PF00400 | 0.441 |
DEG_APCC_DBOX_1 | 198 | 206 | PF00400 | 0.429 |
DEG_SPOP_SBC_1 | 239 | 243 | PF00917 | 0.607 |
DEG_SPOP_SBC_1 | 309 | 313 | PF00917 | 0.565 |
DEG_SPOP_SBC_1 | 329 | 333 | PF00917 | 0.350 |
DEG_SPOP_SBC_1 | 381 | 385 | PF00917 | 0.379 |
DEG_SPOP_SBC_1 | 74 | 78 | PF00917 | 0.610 |
DOC_CYCLIN_RxL_1 | 400 | 411 | PF00134 | 0.500 |
DOC_CYCLIN_yCln2_LP_2 | 190 | 196 | PF00134 | 0.525 |
DOC_MAPK_gen_1 | 209 | 216 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 499 | 507 | PF00069 | 0.654 |
DOC_MAPK_MEF2A_6 | 188 | 196 | PF00069 | 0.429 |
DOC_MAPK_MEF2A_6 | 501 | 509 | PF00069 | 0.517 |
DOC_PP1_SILK_1 | 266 | 271 | PF00149 | 0.562 |
DOC_PP2B_LxvP_1 | 190 | 193 | PF13499 | 0.526 |
DOC_PP2B_LxvP_1 | 542 | 545 | PF13499 | 0.474 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.705 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.532 |
LIG_14-3-3_CanoR_1 | 11 | 17 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 176 | 183 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 284 | 293 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 295 | 301 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 318 | 324 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 440 | 444 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 96 | 102 | PF00244 | 0.608 |
LIG_Actin_WH2_2 | 37 | 54 | PF00022 | 0.541 |
LIG_Actin_WH2_2 | 421 | 439 | PF00022 | 0.562 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.655 |
LIG_BIR_III_2 | 90 | 94 | PF00653 | 0.492 |
LIG_BIR_III_4 | 72 | 76 | PF00653 | 0.507 |
LIG_BRCT_BRCA1_1 | 296 | 300 | PF00533 | 0.513 |
LIG_BRCT_BRCA1_1 | 312 | 316 | PF00533 | 0.513 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.664 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.490 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.491 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.452 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.671 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.633 |
LIG_LIR_Apic_2 | 396 | 401 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 175 | 185 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 384 | 395 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.379 |
LIG_SH2_CRK | 177 | 181 | PF00017 | 0.528 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.547 |
LIG_SH2_PTP2 | 387 | 390 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.547 |
LIG_SH2_STAT3 | 221 | 224 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.379 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.540 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.582 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.443 |
LIG_SUMO_SIM_anti_2 | 100 | 105 | PF11976 | 0.425 |
LIG_SUMO_SIM_anti_2 | 339 | 347 | PF11976 | 0.585 |
LIG_SxIP_EBH_1 | 23 | 32 | PF03271 | 0.589 |
LIG_TRAF2_1 | 120 | 123 | PF00917 | 0.595 |
LIG_TRAF2_1 | 447 | 450 | PF00917 | 0.691 |
LIG_WRC_WIRS_1 | 484 | 489 | PF05994 | 0.413 |
LIG_WW_1 | 35 | 38 | PF00397 | 0.620 |
MOD_CDK_SPK_2 | 427 | 432 | PF00069 | 0.562 |
MOD_CDK_SPxxK_3 | 25 | 32 | PF00069 | 0.645 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.585 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.513 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.461 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.577 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.557 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.573 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.710 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.526 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.597 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.755 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.605 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.644 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.351 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.335 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.319 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.329 |
MOD_GlcNHglycan | 372 | 376 | PF01048 | 0.368 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.732 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.471 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.790 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.771 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.730 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.493 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.572 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.430 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.558 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.461 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.768 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.559 |
MOD_N-GLC_1 | 359 | 364 | PF02516 | 0.326 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.635 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.554 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.453 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.468 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.745 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.511 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.561 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.522 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.487 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.577 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.605 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.607 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.600 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.461 |
MOD_Plk_1 | 377 | 383 | PF00069 | 0.585 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.772 |
MOD_Plk_1 | 503 | 509 | PF00069 | 0.509 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.565 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.519 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.410 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.688 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.594 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.595 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.532 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.379 |
TRG_ER_diArg_1 | 494 | 496 | PF00400 | 0.603 |
TRG_NLS_MonoCore_2 | 167 | 172 | PF00514 | 0.393 |
TRG_NLS_MonoExtN_4 | 165 | 172 | PF00514 | 0.665 |
TRG_Pf-PMV_PEXEL_1 | 227 | 231 | PF00026 | 0.577 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3C1 | Leptomonas seymouri | 49% | 100% |
A0A1X0NKH6 | Trypanosomatidae | 30% | 100% |
A0A3R7KE58 | Trypanosoma rangeli | 32% | 100% |
A0A3S5H5Q8 | Leishmania donovani | 88% | 100% |
A4H4L6 | Leishmania braziliensis | 71% | 100% |
A4HSU2 | Leishmania infantum | 88% | 100% |
C9ZTF4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
Q4QJ28 | Leishmania major | 89% | 100% |
V5BT12 | Trypanosoma cruzi | 31% | 100% |